EP0514067A1 - Composition cosmétique - Google Patents

Composition cosmétique Download PDF

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Publication number
EP0514067A1
EP0514067A1 EP19920304041 EP92304041A EP0514067A1 EP 0514067 A1 EP0514067 A1 EP 0514067A1 EP 19920304041 EP19920304041 EP 19920304041 EP 92304041 A EP92304041 A EP 92304041A EP 0514067 A1 EP0514067 A1 EP 0514067A1
Authority
EP
European Patent Office
Prior art keywords
skin
composition according
citric acid
group
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP19920304041
Other languages
German (de)
English (en)
Other versions
EP0514067B1 (fr
EP0514067B2 (fr
Inventor
Govindrajan Raman
Collur Visweswaria Natraj
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unilever PLC
Unilever NV
Original Assignee
Unilever PLC
Unilever NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Publication of EP0514067A1 publication Critical patent/EP0514067A1/fr
Publication of EP0514067B1 publication Critical patent/EP0514067B1/fr
Application granted granted Critical
Publication of EP0514067B2 publication Critical patent/EP0514067B2/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37—Esters of carboxylic acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/29—Titanium; Compounds thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41—Particular ingredients further characterized by their size
    • A61K2800/413—Nanosized, i.e. having sizes below 100 nm

Definitions

  • the invention relates to a composition for topical application to human skin in order to promote the repair of photo-damaged skin and/or to reduce or prevent the damaging effects of ultra-violet light on skin.
  • the invention also relates to the use of such compositions in the repair of photo-damaged skin and in the prevention of damage to skin due to exposure to ultra-violet light.
  • Skin blotchiness or mottling which accompanies photo-ageing results from changes in the melanocytes within the population of epidermal cells.
  • These pigment producing cells which unlike the keratinocytes remain at the base of the epidermis, lose their normal regulation process with ageing and produce excess pigment. This leads to the formation of dense perinuclear clumps of melanin in slowly turning over keratinocytes within the epidermis, and areas of hyperpigmentation or 'age spots' develop.
  • certain skin lightening agents such as kojic acid, hydroquinone or ascorbic acid are effective by inhibiting the formation of melanin.
  • Vitamin A acid retinoic acid
  • Vitamin A acid is beneficial in hyperpigmentation problems by normalising the melanocyte population.
  • Vitamin A acid prevents accumulation of pigment within the more rapidly dividing and migrating keratinocytes. Vitamin A acid also enhances the pigment reducing potential of conventional skin lightening agents.
  • Vitamin A acid does however have a major drawback in that it is a skin irritant, and can accordingly damage the skin. Its recommended use for example as a prescription drug in the treatment of acne involves careful control, such that excessive doses are avoided in order to restrict the side effects which can occur with skin. By the same token, the use of Vitamin A acid in the treatment or prevention of photo-damaged skin is severely limited by these side effects.
  • esters of citric acid especially tributyl citrate are particularly effective in this respect.
  • Use of such esters is advantageous since they have a history of safe use, for example as plasticizers, including in plastics as used in intravenous fluid tubings.
  • the invention is accordingly concerned with the use of esters of citric acid in the treatment of photo-damaged and/or hyperpigmented skin, and in slowing down the ageing process generally.
  • the invention also concerns compositions for topical application to human skin to reduce damaging effects of ultra-violet light on skin, comprising a citric acid ester in combination with a sunscreen material.
  • the invention provides a composition suitable for topical application to human skin in order to reduce the damaging effects of ultra-violet light on skin, which composition comprises:
  • the present invention provides use of a triester of citric acid having the structure (1) as defined above as an agent for reducing the damaging effects of ultraviolet light on skin, in a topical composition comprising a major proportion of a cosmetically acceptable vehicle for the ester of citric acid.
  • the invention concerns a composition
  • a composition comprising an organic ester of citric acid, together with a suitable cosmetically acceptable vehicle and a sunscreen agent, which acts to retard the ageing process of the skin, when applied topically thereto.
  • the sunscreen agent in the composition assists to prevent skin blotchiness and mottling due to hyperpigmentation and generally effect an overall improvement in skin texture with reduction in fine wrinkling and improved skin colour.
  • Co-formulation with a sunscreen is also believed to enhance synergistically the photo-stability and activity of the ester of citric acid within the formulation and also prevent further actinic damage to all epidermal cells and dermal tissue.
  • composition according to the invention comprises a triester of citric acid or mixtures thereof, each having the structure (1).
  • the preferred esters of citric acid are those where the R1, R2 and R3 groups in structure (1) are each alkyl groups, examples of which include: trimethyl citrate triethyl citrate tri-n-propyl citrate tri-n-butyl citrate trihexyl citrate trioctyl citrate tridodecyl citrate trihexadecyl citrate triphenyl citrate tri-2-ethylhexyl citrate.
  • the above preferred trialkyl citrates can also be acylated at the 2 position, further to enhance their lipophilic character, and examples of these are: 2-acetyl trimethyl citrate 2-acetyl triethyl citrate 2-acetyl tri-n-propyl citrate 2-acetyl tri-n-butyl citrate 2-oleoyl tri-n-butyl citrate 2-0-methyl tri-n-butyl citrate 2-0-ethyl tri-n-butyl citrate 2-0-isopropyl tri-n-butyl citrate.
  • the most preferred citrates are those in which R4 is an acyl group having from 2 to 4 carbon atoms, or an alkyl group having from 1 to 4 carbon atoms.
  • the most preferred ester of citric acid is tri-n-butyl citrate or its acylated derivative.
  • the amount of the ester of citric acid having the structure (1), present in the composition according to the invention is from 0.01 to 20%, particularly from 0.1 to 10% 5 by weight of the composition, preferably more than 0.5%, most preferably at least 1% and typically less than 6%.
  • composition according to the invention also comprises a cosmetically acceptable vehicle to act as a dilutant, dispersant or carrier for other materials present in the composition, so as to facilitate their distribution when the composition is applied to the skin.
  • Vehicles other than water can include liquid or solid emollients, solvents, humectants, thickeners and powders.
  • Emollients such as stearyl alcohol, glyceryl monoricinoleate, mink oil, cetyl alcohol, isopropyl isostearate, stearic acid, isobutyl palmitate, isocetyl stearate, oleyl alcohol, isopropyl laurate, hexyl laurate, decyl oleate, octadecan-2-ol, isocetyl alcohol, eicosanyl alcohol, behenyl alcohol, cetyl palmitate, silicone oils such as dimethylpolysiloxane, di-n-butyl sebacate, isopropyl myristate, isopropyl palmitate, isopropyl stearate,
  • the cosmetically acceptable vehicle will usually form from 10 to 99.9%, preferably from 50 to 99% by weight of the emulsion, and can, in the absence of other cosmetic adjuncts, form the balance of the composition.
  • composition of the invention includes an effective amount of a sunscreen agent which may comprise an organic sunscreen further to enhance synergistically the benefit of the composition in providing protection from the harmful effects of excessive exposure to sunlight.
  • a sunscreen agent which may comprise an organic sunscreen further to enhance synergistically the benefit of the composition in providing protection from the harmful effects of excessive exposure to sunlight.
  • Suitable organic sunscreens when required, include those set out in Table 1 below, and mixtures thereof.
  • composition of the invention can accordingly comprise from 0.1 to 10%, preferably from 1 to 5%, suitably 1.5 to 4.5% by weight of an organic sunscreen material.
  • the sunscreen agent according to the invention can optionally comprise an inorganic sunscreen, such as ultrafine titanium dioxide in either of two forms, namely water-dispersible titanium dioxide and oil-dispersible titanium dioxide.
  • an inorganic sunscreen such as ultrafine titanium dioxide in either of two forms, namely water-dispersible titanium dioxide and oil-dispersible titanium dioxide.
  • Water-dispersible titanium dioxide is ultrafine titanium dioxide, the particles of which are uncoated or which are coated with a material to impart a hydrophilic surface property to the particles.
  • a material to impart a hydrophilic surface property examples include aluminium oxide and aluminium silicate.
  • Oil-dispersible titanium dioxide is ultrafine titanium dioxide, the particles of which exhibit a hydrophobic surface property, and which, for this purpose, can be coated with metal soaps such as aluminium stearate, aluminium laurate or zinc stearate, or with organosilicone compounds.
  • ultra titanium dioxide particles of titanium dioxide having an average particle size of less than 100nm, preferably 70nm or less, more preferably from 10 to 40nm and most preferably from 15 to 25nm.
  • the weight ratio of water-dispersible titanium dioxide to oil-dispersible titanium dioxide should be from 1:4 to 4:1, preferably from 1:2 to 2:1 and ideally about equal weight proportions.
  • the total amount of titanium dioxide that can optionally can be incorporated in the composition according to the invention is from 1 to 25%, preferably from 2 to 10% and ideally from 3 to 7% by weight of the composition.
  • the emulsion of the invention optionally can comprise an inorganic sunscreen in addition to ultrafine titanium dioxide as herein defined.
  • the inorganic sunscreen has an average particle size of less then 70nm, preferably from 10 to 40 nm and most preferably from 15 to 25nm.
  • examples of other inorganic sunscreens include: zinc oxide, iron oxide, and silica, such as fumed silica, having an average particle size of less than 100nm, typically from 1nm to 100nm.
  • silica when used as an ingredient in the emulsion according to the invention can provide protection from infra-red radiation.
  • the composition includes from 1 to 25%, typically from 2 to 10% and most preferably from 3 to 7% by weight of inorganic sunscreens.
  • composition according to the invention is an emulsion, in which case an oil or oily material will normally be present, together with an emulsifier to provide either a water-in-oil emulsion or an oil-in-water emulsion, depending largely on the average hydrophilic-lyophilic balance (HLB) of the emulsifier employed.
  • HLB hydrophilic-lyophilic balance
  • composition according to the invention can optionally comprise one or more oils or other materials having the properties of an oil.
  • oils examples include mineral oil and vegetable oils, and oil materials, such as those already proposed herein as emollients.
  • oils or oily materials include silicone oils, both volatile and non-volatile, such as polydimethyl siloxanes.
  • Oily vehicles in which the esters are soluble or miscible, such that a composition is formed which does not separate into two or more phases on standing are particularly advantageous. In such compositions penetration of the citric acid ester into the skin can thereby be expected to be enhanced.
  • the oil or oily material when present for the purposes for forming an emulsion, will normally form up to 90%, preferably from 10 to 80% by volume of the composition.
  • composition according to the invention can also optionally comprise one or more emulsifiers the choice of which will normally determine whether a water-in-oil or and oil-in-water emulsion is formed.
  • the chosen emulsifier or emulsifiers should normally have an average HLB value of from 1 to 6.
  • a chosen emulsifier or emulsifiers should have an average HLB value of >6.
  • Suitable emulsifiers are set below in Table 1 in which the chemical name of the emulsifiers is given together with an example of a trade name as commercially available, and the average HLB value.
  • the amount of emulsifier or mixtures thereof, that optionally can be incorporated in the composition of the invention is from 1 to 50%, preferably from 2 to 20% and most preferably from 2 to 10% by weight of the composition.
  • composition of the invention can also comprise water, usually up to 80%, preferably from 5 to 80% by volume.
  • composition of the invention can also optionally comprise a high molecular weight silicone surfactant which can also act as an emulsifier, in place of or in addition to the optional emulsifier(s) already mentioned.
  • a high molecular weight silicone surfactant which can also act as an emulsifier, in place of or in addition to the optional emulsifier(s) already mentioned.
  • the silicone surfactant is a high molecular weight polymer of dimethyl polysiloxane with polyoxyethylene and/or polyoxypropylene side chains having a molecular weight of from 10,000 to 50,000 and having the structure: where the groups R′ and R ⁇ are each chosen from -H, C1 ⁇ 18 alkyl and - [CH2 CH2 O] a
  • the dimethyl polysiloxane polymer is one in which:
  • a particularly preferred dimethyl polysiloxane polymer is one in which:
  • the dimethyl polysiloxane polymer is conveniently provided as a dispersion in a volatile siloxane, the dispersion comprising, for example, from 1 to 20% by volume of the polymer and from 80 to 99% by volume of the volatile siloxane.
  • the dispersion consists of a 10% by volume of the polymer dispersed in the volatile siloxane.
  • volatile siloxanes in which the polysiloxane polymer can be dispersed include polydimethyl siloxane (pentamer and/or hexamer).
  • a particularly preferred silicone surfactant is cyclomethicone and dimethicone copolyol, such as DC 3225C Formulation Aid available from DOW CORNING.
  • Another is laurylmethicone copolyol, such as DC Q2-5200, also available from Dow Corning.
  • the amount of silicone surfactant, when present in the composition will normally be up to 25%, preferably from 0.5 to 15% by weight of the emulsion.
  • composition according to the invention optionally can also comprise an additional anti-ageing active such as retinol (Vitamin A) and/or derivative thereof, further to enhance repair of photo damage to skin following exposure to ultra-violet light.
  • an additional anti-ageing active such as retinol (Vitamin A) and/or derivative thereof, further to enhance repair of photo damage to skin following exposure to ultra-violet light.
  • examples of derivatives of retinol include: Retinyl acetate Retinyl butyrate Retinyl propionate Retinyl octanoate Retinyl laurate Retinyl palmitate Retinyl oleate, and Retinyl linoleate.
  • the amount of retinol, or a cosmetically acceptable derivative thereof, when present in the composition according to the invention is from 0.01 to 10% and preferably 0.1 to 5% by weight of the composition.
  • composition according to the invention optionally can also comprise a tocopherol (vitamin E group), as an antioxidant for retinol, or a derivative, when present in the composition, and to limit oxidative damage to skin.
  • vitamin E group comprises ⁇ -tocopherol, ⁇ -tocopherol, ⁇ -tocopherol and ⁇ -tocopherol.
  • the amount of a tocopherol, when present in the composition according to the invention, is from 0.0001 to 20%, preferably from 0.001 to 10% by weight of the composition.
  • adjuncts examples include preservatives, such as para-hydroxy benzoate esters; antioxidants, such butyl hydroxy toluene; humectants, such as glycerol, sorbitol, 2-pyrrolidone-5-carboxylate, dibutylphthalate, gelatin, polyethylene glycol, such as PEG 200-600; buffers, such as lactic acid together with a base such as triethanolamine or sodium hydroxide; waxes, such as beeswax, ozokerite wax, paraffin wax; plant extracts, such as Aloe vera, cornflower, witch hazel, elderflower, cucumber; thickeners; activity enhancers; colourants; and perfumes.
  • Cosmetic adjuncts can form the balance of the composition.
  • the composition according to the invention is intended primarily as a skin care product for topical application to human skin to prevent photo-damage to skin, which can result from exposure to sunlight, and which can retard natural skin ageing.
  • the composition can also be used to reduce skin blotchiness and mottling due to hyperpigmentation, to improve skin texture with reduction in fine wrinkling and otherwise to improve skin colour and texture.
  • the composition when topically applied to skin, is useful in the prevention of actinic damage to all epidermal cells and dermal tissue.
  • a small quantity of the composition for example from 1 to 5ml, is applied to exposed areas of the skin, from a suitable container or applicator and, if necessary, it is then spread over and/or rubbed into the skin using the hand or fingers or a suitable device.
  • the topical skin treatment composition of the invention can be formulated as a lotion having a viscosity of from 4,000 to 10,000 mPas, a fluid cream having a viscosity of from 10,000 to 20,000 mPas or a cream having a viscosity of from 20,000 to 100,000 mPas, or above.
  • the composition can be packaged in a suitable container to suit its viscosity and intended use by the consumer.
  • a lotion or fluid cream can be packaged in a bottle or a roll-ball applicator or a propellant-driven aerosol device or a container fitted with a pump suitable for finger operation.
  • the composition When the composition is a cream, it can simply be stored in a non-deformable bottle or squeeze container, such as a tube or a lidded jar.
  • the invention accordingly also provides a closed container containing a cosmetically acceptable composition as herein defined.
  • a base composition (cream) was prepared as a vehicle for retinoic acid, retinol or tri-n-butyl citrate, to study changes to skin, if any, attributable to these substances.
  • the base composition (cream) contained the following ingredients:
  • Test creams were then prepared by addition to the base cream of retinoic acid, retinol or tri-n-butyl citrate.
  • the test and control (i.e. no additives) creams were applied to the depilated backs of albino mice, albino guinea pigs and black mice (50 mg per animal per application). A total of from 4 to 30 applications were made. Evaluations were performed at the end of the treatment periods by gross morphology and microscopic anatomy. The results are tabulated below:
  • Tri-n-butyl citrate caused histological changes in the epidermis that were similar to that caused by retinol. This indicates that the effects would be beneficial and that tri-n-butyl citrate would have antiageing properties. No irritant effects were observed even on prolonged application.
  • the invention is further illustrated by the following examples; in each formulation, the titanium dioxide employed was ultrafine titanium dioxide having a mean particle size of from 15 to 25nm.
  • This example illustrates a lotion according to the invention.
  • This example illustrates a fluid cream according to the invention.
  • This example illustrates a cream according to the invention.
  • This example illustrates a lotion according to the invention.
  • This example illustrates a cream in accordance with the invention.
  • This example also illustrates a cream in accordance with the invention.
  • This example illustrates a lotion according to the invention.
  • This example illustrates a lotion according to the invention.
  • This example illustrates a lotion according to the invention.
  • This example illustrates an anhydrous formulation for addition of sunscreen in accordance with the invention.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nanotechnology (AREA)
  • Epidemiology (AREA)
  • Birds (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Molecular Biology (AREA)
  • Dermatology (AREA)
  • Medicinal Chemistry (AREA)
  • Medical Informatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Inorganic Chemistry (AREA)
  • Biophysics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
EP92304041A 1991-05-07 1992-05-05 Composition cosmétique Expired - Lifetime EP0514067B2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9109965 1991-05-07
GB919109965A GB9109965D0 (en) 1991-05-07 1991-05-07 Cosmetic composition

Publications (3)

Publication Number Publication Date
EP0514067A1 true EP0514067A1 (fr) 1992-11-19
EP0514067B1 EP0514067B1 (fr) 1997-08-27
EP0514067B2 EP0514067B2 (fr) 2004-07-14

Family

ID=10694655

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92304041A Expired - Lifetime EP0514067B2 (fr) 1991-05-07 1992-05-05 Composition cosmétique

Country Status (11)

Country Link
US (1) US5244665A (fr)
EP (1) EP0514067B2 (fr)
JP (1) JPH0737376B2 (fr)
AT (1) ATE157245T1 (fr)
AU (1) AU652047B2 (fr)
BR (1) BR9201698A (fr)
CA (1) CA2067888C (fr)
DE (1) DE69221766T3 (fr)
ES (1) ES2106828T5 (fr)
GB (1) GB9109965D0 (fr)
ZA (1) ZA923312B (fr)

Cited By (11)

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EP0691126A1 (fr) * 1994-07-05 1996-01-10 Beiersdorf Aktiengesellschaft Compositions cosmétiques ou dermatologiques contenant alpha-hydroxy acides et/ou acides cétoniques et pigments inorganiques
WO1996003110A1 (fr) * 1994-07-22 1996-02-08 Coletica Acide hydroxyle lipophile, son utilisation en cosmetique et en pharmacie, et son procede de preparation
WO1996038125A1 (fr) * 1995-06-02 1996-12-05 Beiersdorf Ag COMPOSITIONS COSMETIQUES OU DERMATOLOGIQUES CONTENANT DES OLIGOMERES OU DES POLYMERES D'ACIDES α-HYDROXYCARBOXYLIQUES
US6013247A (en) * 1996-07-29 2000-01-11 L'oreal Composition for protecting the skin or the hair, containing nanopigments and a solid elastomeric polyorganosiloxane combined with a fatty phase
EP0987005A2 (fr) * 1998-09-18 2000-03-22 Beiersdorf Aktiengesellschaft Systèmes en dispersion fine, sans émulsifiants, de type huile-dans-eau ou eau-dans-huile
US6080390A (en) * 1997-08-27 2000-06-27 Revlon Consumer Products Corporation Moisturizing cosmetic stick compositions
WO2000061078A2 (fr) * 1999-04-10 2000-10-19 Cognis Deutschland Gmbh Agents photoprotecteurs
WO2003075880A1 (fr) * 2002-03-11 2003-09-18 Unilever Plc Compositions cosmetiques renfermant des triesters d'acide citrique
WO2008063441A2 (fr) * 2006-11-16 2008-05-29 The Procter & Gamble Company Composition pour soins personnels
US10245220B2 (en) 2015-07-22 2019-04-02 Biosynthis Process for pongamol enrichment of karanja oil
US20200289382A1 (en) * 2017-09-11 2020-09-17 Oleon Nv Emulsifying combination for obtaining low viscosity water-in-oil emulsions

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US5733531A (en) * 1991-02-05 1998-03-31 Sunsmart, Inc. Composite UV sunblock compositions
EP0608433B1 (fr) * 1992-07-13 2004-05-19 Shiseido Company, Ltd. Composition de preparation dermatologique
JP3566739B2 (ja) * 1993-09-30 2004-09-15 三省製薬株式会社 皮膚外用剤の安定化方法
US6068834A (en) 1994-03-04 2000-05-30 The Procter & Gamble Company Skin lightening compositions
US5451405A (en) * 1994-04-25 1995-09-19 Chesebrough-Pond's Usa Co. Skin treatment composition
CA2130967C (fr) * 1994-08-26 2003-10-28 Dorothy Mccuaig Composition desodorisante a longue duree de vie
US5874463A (en) 1994-10-24 1999-02-23 Ancira; Margaret Hydroxy-kojic acid skin peel
ES2177680T3 (es) * 1994-12-20 2002-12-16 Oreal Composicion de maquillaje revitalizante.
US5618850A (en) * 1995-03-09 1997-04-08 Focal, Inc. Hydroxy-acid cosmetics
FR2735688B1 (fr) * 1995-06-26 1997-08-14 Oreal Utilisation en association d'un alpha-hydroxyacide et d'un oxyde de titane pour le blanchiment de la peau
US5571518A (en) 1995-10-30 1996-11-05 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Cosmetic compositions containing tricholine citrate
US5725845A (en) * 1995-11-03 1998-03-10 Revlon Consumer Products Corporation Transfer resistant cosmetic stick compositions with semi-matte finish
US5690918A (en) * 1995-12-19 1997-11-25 Maybelline, Inc. Solvent-based non-drying lipstick
US5885595A (en) * 1996-05-13 1999-03-23 Elizabeth Arden Co., Division Of Conopco, Inc. Cosmetic composition with a retinol fatty acid ester
US5855877A (en) * 1996-09-06 1999-01-05 Colgate-Palmolive Company Non-aqueous antiperspirant composition
US5874094A (en) * 1997-08-05 1999-02-23 Costello; Jeremiah Cream formulation for topical application
US20030124153A1 (en) * 1997-08-27 2003-07-03 Revlon Consumer Products Corporation Cosmetic Stick Compositions With Improved Application
US6217852B1 (en) * 1998-08-15 2001-04-17 Skinnovative Dermatologic Concepts, L.L.C. Personal cleansing compositions having photoprotective agents
US6165450A (en) * 1999-05-03 2000-12-26 Em Industries, Inc. Sprayable sunscreen compositions
DE10000210A1 (de) * 2000-01-05 2001-07-12 Beiersdorf Ag Kosmetische oder dermatologische Zubereitungen vom Typ Öl-in-Wasser
US6355280B1 (en) * 2000-02-28 2002-03-12 I.M.S. Cosmetics Composition for reducing cell apoptosis containing avocado and soybean lipid unsaponifiables
JP4406855B2 (ja) * 2000-03-17 2010-02-03 株式会社ビメーク 化粧料
US20070166255A1 (en) * 2004-11-22 2007-07-19 Gupta Shyam K Treatment of Topical Discomforts Including Acne, Sunburn, Diaper Rash, Wound, Wrinkles and Dandruff/Hair Loss by Natural Lignans via Fatty Acid Desaturase Inhibition
CN101123937B (zh) * 2005-09-09 2012-10-31 宝洁公司 包含多层的固体护肤组合物
US20080160097A1 (en) 2006-12-28 2008-07-03 Avon Products, Inc. Method for imparting a cosmetic or therapeutic benefit to a topical surface and process for making
WO2015145464A2 (fr) * 2014-03-27 2015-10-01 Kancor Ingredients Ltd Composition d'écran solaire photostable pour application topique

Citations (4)

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EP0691126A1 (fr) * 1994-07-05 1996-01-10 Beiersdorf Aktiengesellschaft Compositions cosmétiques ou dermatologiques contenant alpha-hydroxy acides et/ou acides cétoniques et pigments inorganiques
US6039961A (en) * 1994-07-22 2000-03-21 Coletica Lipophilic hydroxylated acid, its use in cosmetics and pharmacy, and its process of preparation
WO1996003110A1 (fr) * 1994-07-22 1996-02-08 Coletica Acide hydroxyle lipophile, son utilisation en cosmetique et en pharmacie, et son procede de preparation
US5869069A (en) * 1994-07-22 1999-02-09 Coletica Lipophilic hydroxylated acid, its use in cosmetics and pharmacy, and its process of preparation
WO1996038125A1 (fr) * 1995-06-02 1996-12-05 Beiersdorf Ag COMPOSITIONS COSMETIQUES OU DERMATOLOGIQUES CONTENANT DES OLIGOMERES OU DES POLYMERES D'ACIDES α-HYDROXYCARBOXYLIQUES
US6261542B1 (en) 1996-07-29 2001-07-17 L'oreal Composition for protecting the skin or the hair, containing nanopigments and a solid elastomeric polyorganosiloxane combined with a fatty phase
US6013247A (en) * 1996-07-29 2000-01-11 L'oreal Composition for protecting the skin or the hair, containing nanopigments and a solid elastomeric polyorganosiloxane combined with a fatty phase
US6080390A (en) * 1997-08-27 2000-06-27 Revlon Consumer Products Corporation Moisturizing cosmetic stick compositions
US6579529B2 (en) 1998-09-18 2003-06-17 Beiersdorf Ag Emulsifier-free finely disperse systems of the oil-in-water and water-in-oil type
US6692755B2 (en) 1998-09-18 2004-02-17 Beiersdorf Ag Emulsifier-free finely disperse systems of the oil-in-water and water-in-oil type
EP0987005A2 (fr) * 1998-09-18 2000-03-22 Beiersdorf Aktiengesellschaft Systèmes en dispersion fine, sans émulsifiants, de type huile-dans-eau ou eau-dans-huile
EP0987005A3 (fr) * 1998-09-18 2001-10-31 Beiersdorf Aktiengesellschaft Systèmes en dispersion fine, sans émulsifiants, de type huile-dans-eau ou eau-dans-huile
WO2000061078A3 (fr) * 1999-04-10 2001-03-29 Cognis Deutschland Gmbh Agents photoprotecteurs
US6569410B1 (en) 1999-04-10 2003-05-27 Cognis Deutschland Gmbh Sun protection compositions containing UV protection factors and esters of hydroxycarboxylic acids and alk(en)yl oligoglycosides
WO2000061078A2 (fr) * 1999-04-10 2000-10-19 Cognis Deutschland Gmbh Agents photoprotecteurs
WO2003075880A1 (fr) * 2002-03-11 2003-09-18 Unilever Plc Compositions cosmetiques renfermant des triesters d'acide citrique
WO2008063441A2 (fr) * 2006-11-16 2008-05-29 The Procter & Gamble Company Composition pour soins personnels
WO2008063441A3 (fr) * 2006-11-16 2008-08-21 Procter & Gamble Composition pour soins personnels
US10245220B2 (en) 2015-07-22 2019-04-02 Biosynthis Process for pongamol enrichment of karanja oil
US20200289382A1 (en) * 2017-09-11 2020-09-17 Oleon Nv Emulsifying combination for obtaining low viscosity water-in-oil emulsions

Also Published As

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ES2106828T3 (es) 1997-11-16
AU652047B2 (en) 1994-08-11
ES2106828T5 (es) 2005-03-16
ZA923312B (en) 1993-11-08
JPH05124946A (ja) 1993-05-21
JPH0737376B2 (ja) 1995-04-26
DE69221766T2 (de) 1998-01-29
CA2067888C (fr) 1997-06-03
AU1599092A (en) 1992-11-12
US5244665A (en) 1993-09-14
ATE157245T1 (de) 1997-09-15
CA2067888A1 (fr) 1992-11-08
EP0514067B1 (fr) 1997-08-27
DE69221766T3 (de) 2004-09-30
DE69221766D1 (de) 1997-10-02
BR9201698A (pt) 1992-12-15
GB9109965D0 (en) 1991-07-03
EP0514067B2 (fr) 2004-07-14

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